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哺乳动物初级纤毛的分子结构通过冷冻电镜断层扫描技术揭示。

The molecular structure of mammalian primary cilia revealed by cryo-electron tomography.

机构信息

Max Planck Institute of Molecular Cell Biology and Genetics, Dresden, Germany.

Institute of Molecular Genetics of the Czech Academy of Sciences, Prague, Czech Republic.

出版信息

Nat Struct Mol Biol. 2020 Dec;27(12):1115-1124. doi: 10.1038/s41594-020-0507-4. Epub 2020 Sep 28.

Abstract

Primary cilia are microtubule-based organelles that are important for signaling and sensing in eukaryotic cells. Unlike the thoroughly studied motile cilia, the three-dimensional architecture and molecular composition of primary cilia are largely unexplored. Yet, studying these aspects is necessary to understand how primary cilia function in health and disease. We developed an enabling method for investigating the structure of primary cilia isolated from MDCK-II cells at molecular resolution by cryo-electron tomography. We show that the textbook '9 + 0' arrangement of microtubule doublets is only present at the primary cilium base. A few microns out, the architecture changes into an unstructured bundle of EB1-decorated microtubules and actin filaments, putting an end to a long debate on the presence or absence of actin filaments in primary cilia. Our work provides a plethora of insights into the molecular structure of primary cilia and offers a methodological framework to study these important organelles.

摘要

原发性纤毛是一种基于微管的细胞器,对于真核细胞中的信号转导和感应非常重要。与研究透彻的运动纤毛不同,原发性纤毛的三维结构和分子组成在很大程度上尚未被探索。然而,研究这些方面对于理解原发性纤毛在健康和疾病中的功能是必要的。我们开发了一种可行的方法,通过低温电子断层扫描来研究从 MDCK-II 细胞中分离的原发性纤毛的结构,实现了分子分辨率的研究。我们表明,教科书上的“9+0”微管二联体排列仅存在于原发性纤毛的基部。几微米之外,结构变为无定形的 EB1 修饰的微管和肌动蛋白丝束,结束了关于原发性纤毛中是否存在肌动蛋白丝的长期争论。我们的工作为原发性纤毛的分子结构提供了大量的见解,并为研究这些重要细胞器提供了方法学框架。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1c6a/7610599/ff35c59428fb/EMS121795-f001.jpg

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